A Cross-Sectional Analysis of APOE Gene Polymorphism and the Risk of Cognitive Impairments in the Alzheimer's Disease Neuroimaging Initiative Study
Year: 2021
Type: article
Abstract: Background: It is inconclusive on how apolipoprotein epsilon (APOE) gene polymorphism is associated with the risk of having mild cognitive impairment (MCI) or Alzheimer's disease (AD). Objectives: To investigate how APOE genotype is associated with the risk of MCI or AD using the data collected from the Alzheimer's Disease Neuroimaging Initiative (ADNI) participants. Methods: A cross-sectional design was used to analyze the baseline data collected from the 1,720 ADNI participants. APOE gene polymorphism was analyzed on how they are related to the risk of cognitive impairments of either MCI or AD using a percent yield (PY) method. Then cognitive functions were compared among six different APOE genotypes using a two-way ANCOVA by controlling possible confounding factors. Results: The prevalence of six APOE genotypes in 1,720 participants is as following: e2/e2 (0.3%), e2/e3 (7.4%), e3/e3 (45.4%), e2/e4 (2%), e3/e4 (35%) and e4/e4 (9.9%). The e2/e2 and e4/e4 genotypes were associated with the lowest and the highest risk respectively for cognitive impairments of either MCI or AD. Further, a worse cognitive diagnosis was associated with an increasing number of APOE e4 allele in a dose dependent manner. Participants with genotype e3/e3 had a better memory measure than those with the genotype of e3/e4. Conclusions: APOE gene polymorphism is associated with different level of risks for cognitive impairments. The heterozygous genotype e3/e4 is associated with a worse memory function compared to the genotype of e3/e3. Further investigations are needed to intervene the cognitive deteriorations in those with at risk APOE genotypes.
Authors: G. Wang, D.E. Vance, W. Li
Language: English
Subfield: Psychiatry and Mental health
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $1,640
Awards: G1104192986, G113062254, G1171648585, G1173778324, Michigan Alzheimer's Disease Core Center, UC Davis Alzheimer's Disease Core Center, Indiana Alzheimer Disease Center, G1375833519, G1492531059, G1614502467, G1663213784, G1778344677, Wake Forest Alzheimer's Disease Core Center, G2075747288, G234895681, University of Kentucky Alzheimer's Disease Core Center, Neurobiology of Alzheimer's Disease and Aging, G2640555407, G2769554943, G3036763132, G3066742295, Alzheimer's Disease Research Center, National Alzheimer's Coordinating Center, UCSD Alzheimer's Disease Research Center P50, G3335858628, G3359100610, G3439557519, Alzheimer's Disease Research Center, G3946457848, G4103239427, Alzheimer's Disease Core Center, G4318823550, The Alzheimer's Disease Research Center at the University of California, Irvine, Stanford Alzheimer's Disease Research Center, G4684857399, Oregon Alzheimer's Disease Center, G496605150, Rush Alzheimer's Disease Core Center, G511679733, Alzheimer's Disease Core Center, Alzheimer's Disease Research Center - Overall, Wisconsin Alzheimer's Disease Research Center, G6492025387, University of Kansas Alzheimer's Disease Core Centers, G6750444795, Alzheimer's Disease Research Center, Alzheimer Disease Research Center, Yale Alzheimer Disease Research Center, Arizona Alzheimer's Disease Core Center, Johns Hopkins Alzheimer's Disease Research Center, G7409097460, Boston University Alzheimer's Disease Center, Alzheimer's Disease Research Center, Massachusetts Alzheimer's Disease Research Center, Alzheimer's Disease Core Center, G8018240826, Emory Alzheimer's Disease Center, University of Florida - Mt. Sinai Medical Center AD Research Center, G873702183, G9000005508, G9000013408, G9000025891, G9000030076, G9000033698, G9000036492, G9000064269, G9000070217, G9000092781, G9000104082, G9000108235, G9000119544, G9000126115, G9000132673, G9000145746, G9000167101, G9000208643, G9000212151, G9000218452, G9000218858, G9000227227, G9000227779, G9000252716, G9000274623, G9000307348, G9000352745, G9000354213, New Approaches to Dementia Heterogeneity, Mayo Alzheimer's Disease Research Center
OpenAlex ID: W3158807147
